Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.
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Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery diseaseRNAi-based functional profiling of loci from blood lipid genome-wide association studies identifies genes with cholesterol-regulatory functionThe impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular diseaseGenetic epidemiology of coronary artery disease: an Asian Indian perspectiveGenetic prediction of common diseases. Still no help for the clinical diabetologist!Genetics of coronary artery diseaseHuman Genetics and the Causal Role of Lipoprotein(a) for Various DiseasesLipoprotein(a) and risk of myocardial infarction--genetic epidemiologic evidence of causalityLarge-scale gene-centric analysis identifies novel variants for coronary artery diseaseCaution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosisA latent variable partial least squares path modeling approach to regional association and polygenic effect with applications to a human obesity studyLarge scale association analysis identifies three susceptibility loci for coronary artery diseaseGenetics of venous thrombosis: insights from a new genome wide association studySystematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of KosraeGenetics and beyond--the transcriptome of human monocytes and disease susceptibilityGenome-wide association study of coronary artery disease in the JapaneseA genome-wide association study of a coronary artery disease risk variantLarge-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.Macrophages in the pathogenesis of atherosclerosisLipoprotein (a) as a cause of cardiovascular disease: insights from epidemiology, genetics, and biologyDetailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.Common genetic variants and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA).Characterization of Ath29, a major mouse atherosclerosis susceptibility locus, and identification of Rcn2 as a novel regulator of cytokine expressionGenetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.Accurate estimation of haplotype frequency from pooled sequencing data and cost-effective identification of rare haplotype carriers by overlapping pool sequencing.Ehapp2: Estimate haplotype frequencies from pooled sequencing data with prior database information.A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.Expression of organic cation transporters OCT1 (SLC22A1) and OCT3 (SLC22A3) is affected by genetic factors and cholestasis in human liver.The interleukin-1 cluster, dyslipidaemia and risk of myocardial infarctionTelomere biology in healthy aging and disease.Effect of diet-induced weight loss on lipoprotein(a) levels in obese individuals with and without type 2 diabetesTowards a molecular systems model of coronary artery diseaseImplications of genetic polymorphisms in inflammation-induced atherosclerosisGenome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiographyGenome-wide association analysis of incident coronary heart disease (CHD) in African Americans: a short reportRecent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk.Lipoprotein(a) levels and long-term cardiovascular risk in the contemporary era of statin therapy.The role of endoplasmic reticulum stress in the progression of atherosclerosis.Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--
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P2860
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Genome-wide haplotype associat ...... s for coronary artery disease.
@en
Genome-wide haplotype associat ...... s for coronary artery disease.
@en-gb
Genome-wide haplotype associat ...... s for coronary artery disease.
@nl
type
label
Genome-wide haplotype associat ...... s for coronary artery disease.
@en
Genome-wide haplotype associat ...... s for coronary artery disease.
@en-gb
Genome-wide haplotype associat ...... s for coronary artery disease.
@nl
prefLabel
Genome-wide haplotype associat ...... s for coronary artery disease.
@en
Genome-wide haplotype associat ...... s for coronary artery disease.
@en-gb
Genome-wide haplotype associat ...... s for coronary artery disease.
@nl
P2093
P2860
P50
P356
P1433
P1476
Genome-wide haplotype associat ...... s for coronary artery disease.
@en
P2093
Alexandru Munteanu
Alun Evans
Anika Grosshennig
Anthony J Balmforth
Arne Schäfer
Ben J Wright
Cardiogenics Consortium
Caroline Morrison
Christian Hengstenberg
Claire Perret
P2860
P2888
P304
P356
10.1038/NG.314
P407
P50
P577
2009-02-08T00:00:00Z
P6179
1024063292